NP-MRD: Showing NP-Card for 21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate (NP0196670)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-04 14:47:51 UTC

Updated at

2022-09-04 14:47:51 UTC

NP-MRD ID

NP0196670

Secondary Accession Numbers

None

Natural Product Identification

Common Name

21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216472D          

 46 52  0  0  0  0            999 V2000
   -2.0954    1.1210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2774    1.2281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7756    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1075   -0.1898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -0.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2437   -0.7802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5366    0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0526    0.6959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4620    1.4492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1752    1.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6631    1.2473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4863    1.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8931    2.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4165    2.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5855    2.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6846    1.6655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4890    1.3058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9715    0.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8153    0.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3560    0.0526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0873   -0.7237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6241   -1.3502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4351   -1.1986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2675   -0.8722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0115   -1.6565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6889   -0.2642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0751   -0.8940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6956   -1.6870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8632   -1.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2861   -2.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5707   -2.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992   -3.1363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9434   -2.5022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7508   -2.6717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3013   -2.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0204   -3.6110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2009   -3.4702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9245   -2.6871    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1102   -2.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4398   -2.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8865   -1.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1764    1.4400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7103    2.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8849    2.0509    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    4.8049    2.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1635    2.4511    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 30 40  1  0  0  0  0
 40 41  1  0  0  0  0
  6 41  1  0  0  0  0
 19 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 17 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
M  CHG  2  44   1  46  -1
M  END

     RDKit          3D

 86 92  0  0  0  0  0  0  0  0999 V2000
   -6.0575   -4.2846    1.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0560   -3.9486    0.8772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8583   -2.6110    0.4990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7069   -1.7015    1.0919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5042   -0.3977    0.7143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5291    0.0353   -0.1980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6980   -0.9123   -0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8846   -2.2028   -0.4069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1189   -3.3466   -0.8505 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6622   -3.2703   -0.8442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9912   -3.3980    0.3098 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4359   -3.2928    0.3872 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1523   -3.0531   -0.7714 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4202   -2.9404   -1.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9923   -3.0462   -2.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6494   -2.8182   -0.7611 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0110   -1.3580   -1.0221 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3834   -0.6321    0.2239 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5377   -1.0319    0.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0100   -0.5025    2.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2705    0.4656    2.6356 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7390    0.9858    3.8265 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9218    0.5938    4.4476 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0843    0.8728    2.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4467    1.8686    2.7916 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5834    0.3763    0.8340 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4460    0.7641    0.2184 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3197    1.4500   -0.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9618    1.3197    0.5332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0461    2.0752    0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8914    3.0437   -0.8269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6737    3.2212   -1.4653 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3683    2.4435   -1.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5764    2.6875   -1.7954 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6541    3.6347   -2.8003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9598    4.0105   -1.2767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1282    4.1485   -0.4148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8726    3.5041    0.8089 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9786    4.2284    1.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4479    2.1085    0.6455 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4867    1.5210   -0.3065 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4408   -2.0441    0.1579 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3560   -1.8582   -1.3302 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1966   -1.2327   -1.8439 N   0  0  1  0  0  4  0  0  0  0  0  0
    3.9857   -1.6676   -3.2089 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4309    0.1037   -1.9160 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.0961   -4.0985    1.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9523   -3.7552    2.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9990   -5.3948    1.9969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4684   -1.9938    1.7986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1868    0.3423    1.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9406   -0.6123   -1.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654   -3.6251    1.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7433   -3.4336    1.4583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7356   -2.7736   -3.0152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4219   -2.9414   -3.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2773   -3.4404   -1.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1492   -3.0371    0.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1750   -0.9392   -1.5878 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9520   -0.8520    2.4624 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8212    0.5844    3.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1238    1.3383    5.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7618   -0.3736    4.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    2.2543    2.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9612    0.4937    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5781    3.9825   -2.2708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3542    4.6166   -2.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6721    3.6284   -3.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9451    3.3565   -3.6244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2854    3.7941   -2.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4291    5.0239   -1.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0435    3.8270   -0.9611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2914    5.2409   -0.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9523    5.3169    1.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3561    4.1387    2.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9357    3.8025    1.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7408    1.7433    1.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5132    1.9255   -0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3262    1.9992   -1.2580 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3272   -3.0575    0.5329 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5176   -1.7876    0.4988 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2250   -1.1695   -1.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6472   -2.7874   -1.8851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109   -1.3182   -3.6327 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1508   -2.7559   -3.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7493   -1.1735   -3.8577 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  1  0
 16 13  1  0
 13 12  2  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6 41  1  0
 41 40  1  0
 40 38  1  0
 38 39  1  0
 38 37  1  0
 37 36  1  0
 36 31  1  0
 31 30  2  0
 30 29  1  0
 29 28  2  0
 28 27  1  0
 27 26  1  0
 26 24  2  0
 24 25  1  0
 28 33  1  0
 33 34  1  0
 34 35  1  0
 33 32  2  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  1  0
 10 15  1  0
 15 14  2  0
 17 44  1  0
 44 45  1  0
 44 46  1  6
 44 43  1  0
 43 42  1  0
 24 21  1  0
 42 19  1  0
 26 18  1  0
 14 13  1  0
  3  8  1  0
 30 40  1  0
 32 31  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 20 60  1  0
 17 59  1  6
 16 57  1  0
 16 58  1  0
 12 54  1  0
 11 53  1  0
  7 52  1  0
 41 78  1  0
 41 79  1  0
 40 77  1  1
 39 74  1  0
 39 75  1  0
 39 76  1  0
 37 72  1  0
 37 73  1  0
 36 70  1  0
 36 71  1  0
 29 65  1  0
 25 64  1  0
 35 67  1  0
 35 68  1  0
 35 69  1  0
 32 66  1  0
  5 51  1  0
  4 50  1  0
  1 47  1  0
  1 48  1  0
  1 49  1  0
 15 56  1  0
 14 55  1  0
 45 84  1  0
 45 85  1  0
 45 86  1  0
 43 82  1  0
 43 83  1  0
 42 80  1  0
 42 81  1  0
M  CHG  2  44   1  46  -1
M  END


  Mrv1652309042216472D          

 46 52  0  0  0  0            999 V2000
   -2.0954    1.1210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2774    1.2281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7756    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1075   -0.1898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -0.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2437   -0.7802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5366    0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0526    0.6959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4620    1.4492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1752    1.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6631    1.2473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4863    1.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8931    2.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4165    2.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5855    2.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6846    1.6655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4890    1.3058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9715    0.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8153    0.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3560    0.0526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0873   -0.7237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6241   -1.3502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4351   -1.1986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2675   -0.8722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0115   -1.6565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6889   -0.2642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0751   -0.8940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6956   -1.6870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8632   -1.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2861   -2.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5707   -2.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992   -3.1363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9434   -2.5022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7508   -2.6717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3013   -2.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0204   -3.6110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2009   -3.4702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9245   -2.6871    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1102   -2.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4398   -2.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8865   -1.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1764    1.4400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7103    2.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8849    2.0509    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    4.8049    2.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1635    2.4511    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 30 40  1  0  0  0  0
 40 41  1  0  0  0  0
  6 41  1  0  0  0  0
 19 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 17 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
M  CHG  2  44   1  46  -1
M  END
> <DATABASE_ID>
NP0196670

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3C(CC4=CC=C(OC5=CC(CC6N(C)CCC7=C6C=C(OC3=C1O)C(OC)=C7)=CC=C5OC)C=C4)[N+](C)([O-])CC2

> <INCHI_IDENTIFIER>
InChI=1S/C37H40N2O7/c1-38-14-12-24-19-31(43-4)33-21-27(24)28(38)16-23-8-11-30(42-3)32(18-23)45-26-9-6-22(7-10-26)17-29-35-25(13-15-39(29,2)41)20-34(44-5)36(40)37(35)46-33/h6-11,18-21,28-29,40H,12-17H2,1-5H3

> <INCHI_KEY>
BMNWTEXRVYGPQW-UHFFFAOYSA-N

> <FORMULA>
C37H40N2O7

> <MOLECULAR_WEIGHT>
624.734

> <EXACT_MASS>
624.283551636

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
66.33156231725471

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{9,12}.1^{3,7}.1^{14,18}.0^{27,31}.0^{22,33}]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate

> <JCHEM_LOGP>
4.909363280845436

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.509057972199432

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.970959569610812

> <JCHEM_PKA_STRONGEST_BASIC>
7.850142036291162

> <JCHEM_POLAR_SURFACE_AREA>
92.68

> <JCHEM_REFRACTIVITY>
177.67719999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{9,12}.1^{3,7}.1^{14,18}.0^{27,31}.0^{22,33}]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.911   2.093   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.384   2.292   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.448   1.070   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.067  -0.354   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.117  -1.594   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.455  -1.456   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.002   0.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.098   1.299   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.862   2.705   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.194   3.606   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.104   2.328   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.641   2.389   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.400   3.747   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.511   5.067   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.960   4.985   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.878   3.109   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.379   2.438   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.280   1.070   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.855   1.278   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.865   0.098   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.363  -1.351   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      12.365  -2.520   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      13.879  -2.237   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.833  -1.628   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.355  -3.092   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.753  -0.493   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.607  -1.669   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.898  -3.149   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.345  -2.924   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.267  -4.074   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.799  -5.555   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.345  -5.854   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.361  -4.671   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.868  -4.987   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.896  -3.840   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.771  -6.740   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.242  -6.478   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0       1.726  -5.016   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0       0.206  -4.769   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.688  -3.781   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.655  -2.537   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      11.529   2.688   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      10.659   3.950   0.000  0.00  0.00           C+0
HETATM   44  N   UNK     0       9.118   3.828   0.000  0.00  0.00           N+1
HETATM   45  C   UNK     0       8.969   5.361   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       7.772   4.575   0.000  0.00  0.00           O-1
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   41                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16   13   17                                                       
CONECT   17   16   18   44                                                  
CONECT   18   17   19   26                                                  
CONECT   19   18   20   42                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   18   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   40                                                  
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   31   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   30   41                                                  
CONECT   41   40    6                                                       
CONECT   42   19   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   17   45   46                                             
CONECT   45   44                                                            
CONECT   46   44                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₀N₂O₇

Average Mass

624.7340 Da

Monoisotopic Mass

624.28355 Da

IUPAC Name

21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{9,12}.1^{3,7}.1^{14,18}.0^{27,31}.0^{22,33}]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3C(CC4=CC=C(OC5=CC(CC6N(C)CCC7=C6C=C(OC3=C1O)C(OC)=C7)=CC=C5OC)C=C4)[N+](C)([O-])CC2

InChI Identifier

InChI=1S/C37H40N2O7/c1-38-14-12-24-19-31(43-4)33-21-27(24)28(38)16-23-8-11-30(42-3)32(18-23)45-26-9-6-22(7-10-26)17-29-35-25(13-15-39(29,2)41)20-34(44-5)36(40)37(35)46-33/h6-11,18-21,28-29,40H,12-17H2,1-5H3

InChI Key

BMNWTEXRVYGPQW-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.91	ChemAxon
pKa (Strongest Acidic)	8.97	ChemAxon
pKa (Strongest Basic)	7.85	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	92.68 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	177.68 m³·mol⁻¹	ChemAxon
Polarizability	66.33 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate (NP0196670)

MOL for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

3D MOL for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

3D SDF for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

3D-SDF for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

PDB for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

3D PDB for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

SMILES for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

INCHI for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

Structure for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)

3D Structure for NP0196670 (21-hydroxy-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.2⁹,¹².1³,⁷.1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,7(36),9,11,18(33),19,21,24(32),25,27(31),34-dodecaen-15-ium-15-olate)